A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695845



Internal ID15085811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61104134..61107733hg38UCSC Ensembl
Innerchr6:58071881..58075480hg19UCSC Ensembl
Innerchr6:58179840..58183439hg18UCSC Ensembl
Innerchr6:58179840..58183439hg17UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383600
hg193600
hg183600
hg173600
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515916
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695845
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer