A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015599



Internal ID19104816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64866653hg38UCSC Ensembl
Innerchr9:69474914..69879071hg19UCSC Ensembl
Innerchr9:68764734..69168891hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38404158
hg19404158
hg18404158
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7656n100
Supporting Variantsnssv3696129, nssv3696128
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015599
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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