A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699197



Internal ID15089163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3019420..3020455hg38UCSC Ensembl
Innerchr6:3019654..3020689hg19UCSC Ensembl
Innerchr6:2964653..2965688hg18UCSC Ensembl
Innerchr6:2964653..2965688hg17UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381036
hg191036
hg181036
hg171036
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523441
Supporting Variants
Samples
Known GenesHTATSF1P2, NQO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699197
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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