A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023603



Internal ID19112820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64813210hg38UCSC Ensembl
Innerchr9:69474914..69825628hg19UCSC Ensembl
Innerchr9:68764734..69115448hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38350715
hg19350715
hg18350715
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7656n100
Supporting Variantsnssv3696124, nssv3696125
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)nsv1023603
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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