A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563707



Internal ID20936778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125606968..134343906hg38UCSC Ensembl
chr6:125928114..134665044hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg388736939
hg198736931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271170
Samples
Known GenesAKAP7, ARG1, ARHGAP18, C6orf58, CENPW, CTAGE9, CTGF, ECHDC1, ENPP1, ENPP3, EPB41L2, EYA4, HEY2, HINT3, HMGA1P7, KIAA0408, L3MBTL3, LAMA2, LINC00326, LINC01013, LOC643623, MED23, MGC34034, MIR5695, MOXD1, NCOA7, OR2A4, PTPRK, RNF146, RPS12, RSPO3, SAMD3, SGK1, SLC18B1, SLC2A12, SMLR1, SNORA33, SNORD100, SNORD101, SOGA3, STX7, TAAR1, TAAR2, TAAR3, TAAR5, TAAR6, TAAR8, TAAR9, TBPL1, TCF21, THEMIS, TMEM200A, TMEM244, TRMT11, VNN1, VNN2, VNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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