A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702949



Internal ID15439601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38457695..38463423hg38UCSC Ensembl
Innerchr7:38497295..38503023hg19UCSC Ensembl
Innerchr7:38463820..38469548hg18UCSC Ensembl
Innerchr7:38270535..38276263hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385729
hg195729
hg185729
hg175729
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526627
Supporting Variants
Samples
Known GenesAMPH
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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