A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271170



Internal ID20838210
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 StatusS
Merged Variantsnsv6563707
Supporting Variants
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)nssv18271170
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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