A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574607



Internal ID20947678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35958610..45735691hg38UCSC Ensembl
chr7:35998220..45775290hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg389777082
hg199777071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275612
Samples
Known GenesADCY1, AEBP1, AMPH, ANLN, AOAH, AOAH-IT1, BLVRA, C7orf10, C7orf25, CAMK2B, CCM2, CDK13, COA1, DBNL, DDX56, EEPD1, ELMO1, ELMO1-AS1, EPDR1, FAM183B, GCK, GLI3, GPR141, H2AFV, HECW1, INHBA, INHBA-AS1, KIAA0895, LINC00265, LINC00957, LOC100506895, LOC101928618, MIR1200, MIR3943, MIR4649, MIR4657, MIR6837, MIR6838, MPLKIP, MRPL32, MRPS24, MYL7, MYO1G, NACAD, NME8, NPC1L1, NUDCD3, OGDH, PGAM2, POLD2, POLM, POLR2J4, POU6F2, POU6F2-AS1, PPIA, PSMA2, PURB, RALA, RAMP3, RASA4CP, SEPT7P2, SFRP4, SNHG15, SNORA5A, SNORA5B, SNORA5C, SNORA9, SPDYE1, STARD3NL, STK17A, TARP, TBRG4, TMED4, TRG-AS1, UBE2D4, URGCP, URGCP-MRPS24, VPS41, YAE1D1, YKT6, ZMIZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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