A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981957



Internal ID12974213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65097016..65452987hg38UCSC Ensembl
Innerchr7:64557394..64917900hg19UCSC Ensembl
Innerchr7:64194829..64555335hg18UCSC Ensembl
Innerchr7:64001544..64362050hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38355972
hg19360507
hg18360507
hg17360507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752168
Supporting Variants
SamplesBEC_508
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981957
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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