A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7104



Internal ID15205394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135256048..135301533hg38UCSC Ensembl
OuterchrX:134389996..134435459hg19UCSC Ensembl
OuterchrX:134217662..134263125hg18UCSC Ensembl
OuterchrX:134115516..134160979hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3845486
hg1945464
hg1845464
hg1745464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6378
SamplesNA12156
Known GenesZNF75D
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7104
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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