A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025153



Internal ID19114371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62992776..63373594hg38UCSC Ensembl
Innerchr7:62453154..62833972hg19UCSC Ensembl
Innerchr7:62090589..62471407hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38380819
hg19380819
hg18380819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6431n100
Supporting Variantsnssv3661959
Samples
Known GenesLOC100287704, LOC100287834, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025153
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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