A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986634



Internal ID12982067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62978903..63376555hg38UCSC Ensembl
Innerchr7:62439281..62836933hg19UCSC Ensembl
Innerchr7:62076716..62474368hg18UCSC Ensembl
Innerchr7:61883431..62281083hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38397653
hg19397653
hg18397653
hg17397653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34968
Supporting Variants
SamplesNA19120
Known GenesLOC100287704, LOC100287834, ZNF733P
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986634
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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